HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378762Generated: October 26, 2026
Sodium hydride → 4-[N,N-bis(3,4-dimethylphenyl)amino]styrene
https://huagongshe.com/reaction/378762
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Trimethylphosphonium bromide | HCID 22062633 | — |
| Reactant | 4-[N,N-bis(3,4-dimethylphenyl)amino]benzaldehyde | HCID 22617091 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-[N,N-bis(3,4-dimethylphenyl)amino]styrene | HCID 10892783 | 85% |
Reaction Steps
Into a three-necked flask, 12.1 g of sodium hydride and 580 ml of 1,2-dimethoxyethane were placed, and 108.5 g of trimethylphosphonium bromide was added thereto with stirring at room temperature. Next, after a drop of absolute alcohol was added, the reaction was allowed to proceed at 70° C. for 4 hours. Then, 100.0 g of 4-[N,N-bis(3,4-dimethylphenyl)amino]benzaldehyde was added to the reaction mixture, to carry out reaction at 700° C. for 5 hours, followed by filtration to collect a cake. The cake was extracted with ether and the extract was put together with the filtrate and washed with water. Then, the ether solution was dehydrated with calcium chloride, and thereafter the ether was removed to obtain a crude product. After twice recrystallized from ethanol, acicular 4-[N,N-bis(3,4-dimethylphenyl)amino]styrene was obtained in an amount of 84.5 g (yield: 85.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06296978B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-84aad4bf4c1a4f86893309f2ba48179e |
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| Source note | uspto-grants-2001_10 |
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